学术探索
学术期刊
新闻热点
数据分析
智能评审

MIDAS SYNDROME RESPECTIVELY MLS SYNDROME - A SEPARATE ENTITY RATHER THAN A PARTICULAR LYONIZATION PATTERN OF THE GENE CAUSING GOLTZ-SYNDROME

被引：21
作者：
MUCKE, J
HAPPLE, R
THEILE, H
机构：
[1] UNIV SAARLAND,INST HUMAN GENET,W-6650 HOMBURG,GERMANY
[2] UNIV MARBURG,DEPT DERMATOL,W-3550 MARBURG,GERMANY
[3] UNIV LEIPZIG,INST HUMAN GENET,O-7010 LEIPZIG,GERMANY
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 57卷 / 01期
关键词：
D O I：
10.1002/ajmg.1320570123
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：117 / 118
页数：2
相关论文
共 3 条
[1]   MIDAS SYNDROME (MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA) - AN X-LINKED PHENOTYPE DISTINCT FROM GOLTZ-SYNDROME [J].
HAPPLE, R ;
DANIELS, O ;
KOOPMAN, RJJ .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (05) :710-713
[2]   MICROPHTHALMIA WITH LINEAR SKIN DEFECTS (MLS) SYNDROME - CLINICAL, CYTOGENETIC, AND MOLECULAR CHARACTERIZATION [J].
LINDSAY, EA ;
GRILLO, A ;
FERRERO, GB ;
ROTH, EJ ;
MAGENIS, E ;
GROMPE, M ;
HULTEN, M ;
GOULD, C ;
BALDINI, A ;
ZOGHBI, HY ;
BALLABIO, A .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 49 (02) :229-234
[3]  
MUCKE J, 1994, IN PRESS EUR J DERMA
1